Target Recognition- and HCR Amplification-Induced In Situ Electrochemical Signal Probe Synthesis Strategy for Trace ctDNA Analysis

An electrochemical-DNA (E-DNA) sensor was constructed by using DNA metallization to produce an electrochemical signal reporter in situ and hybridization chain reaction (HCR) as signal amplification strategy. The cyclic voltammetry (CV) technique was used to characterize the electrochemical solid-state Ag/AgCl process. Moreover, the enzyme cleavage technique was introduced to reduce background signals and further improve recognition accuracy. On the basis of these techniques, the as-prepared E-DNA sensor exhibited superior sensing performance for trace ctDNA analysis with a detection range of 0.5 fM to 10 pM and a detection limit of 7 aM. The proposed E-DNA sensor also displayed excellent selectivity, satisfied repeatability and stability, and had good recovery, all of which supports its potential applications for future clinical sample analysis.

Automated summary

An electrochemical-DNA (E-DNA) sensor was developed using DNA metallization as a signal reporter and hybridization chain reaction (HCR) as a signal amplification strategy. The sensor demonstrated superior sensing performance for trace ctDNA analysis, with a wide detection range and low detection limit. It also showed excellent selectivity, repeatability, stability, and recovery, making it a promising tool for clinical sample analysis.